Recurrent Cerebrovascular Complications under Enzyme Replacement Therapy in a Patient with Fabry Disease on Peritoneal Dialysis
Author:
Affiliation:
1. Department of Nephrology, Nagoya University Graduate School of Medicine, Japan
2. Chubu Rosai Hospital, Japan
3. Masuko Memorial Hospital, Japan
4. Department of Nephrology and Rheumatology, Aichi Medical University, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/62/4/62_0185-22/_pdf
Reference18 articles.
1. 1. Robert JH, Bissler J, Banikazemi M, et al. Characterization of Fabry disease in 352 pediatric patients in the Fabry Registry. Pediatr Res 5: 550-555, 2008.
2. 2. Sawada J, Nakagawa N, Kano K, et al. Characteristics of neurological symptoms in adult Japanese patients with Fabry disease. Intern Med 60: 1819-1826, 2021.
3. 3. Mignani R, Feriozzi S, Schaefer RM, et al. Dialysis and transplantation in Fabry disease: indications for enzyme replacement therapy. Clin J Am Soc Nephrol 5: 379-385, 2010.
4. 4. Sakuraba H, Togawa T, Takahiro T, Kato H. Plasma lyso-Gb3: a biomarker for monitoring fabry patients during enzyme replacement therapy. Clin Exp Nephrol 22: 843-849, 2018.
5. 5. Arends M, Wijburg FA, Wanner C, et al. Favourable effect of early versus late start of enzyme replacement therapy on plasma globotriaosylsphingosine levels in men with classical Fabry disease. Mol Genet Metab 121: 157-161, 2017.
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1. An Overview of Molecular Mechanisms in Fabry Disease;Biomolecules;2022-10-12
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